A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502198



Internal ID20875441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58893201..58893900hg38UCSC Ensembl
chr15:59185400..59186099hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026200
Samples
Known GenesSLTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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